{"title":"一项真实试验研究,评估勃起功能障碍患者对阿伐那非治疗的满意度。","authors":"Ping-Ju Tsai, Shih-Ya Hung, Tsung-Hsi Lee, Bang-Ping Jiann","doi":"10.1093/sexmed/qfae001","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Avanafil is a second-generation phosphodiesterase type 5 (PDE5) inhibitor, and offers a rapid onset of action (15 minutes). Its real-world data, including treatment satisfaction, are still lacking.</p><p><strong>Aim: </strong>The study sought to investigate the treatment outcomes of avanafil and the factors impacting treatment satisfaction in a real-world setting.</p><p><strong>Methods: </strong>Between November 2021 and February 2023, erectile dysfunction (ED) patients prescribed avanafil were consecutively enrolled in this phase 4, open-label, cross-sectional, observational study. At each follow-up visit (4-week intervals), participants completed a questionnaire for assessing the use and treatment-emergent adverse events of avanafil, ED severity, and treatment satisfaction.</p><p><strong>Outcomes: </strong>The outcome measures included the Sexual Health Inventory for Men (SHIM), and Erectile Dysfunction Inventory of Treatment Satisfaction.</p><p><strong>Results: </strong>Among 234 patients enrolled, 112 (47.9%) patients had follow-up visits and answered the questionnaire. Treatment with avanafil significantly improved the mean SHIM total score from 10.2 ± 5.6 at baseline to 17.5 ± 6.2 (<i>P</i> < .001). Of the patients treated with avanafil, 71.4% (n = 80 of 112) reported a >4-point improvement in the SHIM total score, and 33.1% (n = 37 of 112) reported normal erectile function. The proportion of patients satisfied with avanafil treatment (defined as Erectile Dysfunction Inventory of Treatment Satisfaction index score ≥60) was 87.5%. Several physical factors (younger age, lower waist circumference, and lower level of low-density lipoprotein), and sexual function factors (shorter duration of ED, higher SHIM total score at baseline, PDE5 inhibitor treatment naive, and acquired premature ejaculation) tended to contribute to satisfaction with avanafil treatment. Treatment-emergent adverse events occurred in 41.1% of patients, and all were mild in severity.</p><p><strong>Clinical implications: </strong>This study identifies the factors associated with treatment satisfaction of avanafil, which may ultimately lead to better treatment outcomes.</p><p><strong>Strengths and limitations: </strong>This is the first study to provide real-world evidence of avanafil for ED treatment, and validated questionnaires were used to assess erectile function and treatment satisfaction. However, the limitations of this study include single-center observational study design, small sample size, and short-term follow-up.</p><p><strong>Conclusion: </strong>Avanafil is an effective treatment for ED, and satisfaction rate is high in an outpatient setting. The awareness of identified factors related to patient satisfaction may improve treatment outcomes.</p>","PeriodicalId":21782,"journal":{"name":"Sexual Medicine","volume":null,"pages":null},"PeriodicalIF":2.6000,"publicationDate":"2024-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10849181/pdf/","citationCount":"0","resultStr":"{\"title\":\"A real-world pilot study assessing treatment satisfaction with avanafil in patients with erectile dysfunction.\",\"authors\":\"Ping-Ju Tsai, Shih-Ya Hung, Tsung-Hsi Lee, Bang-Ping Jiann\",\"doi\":\"10.1093/sexmed/qfae001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Avanafil is a second-generation phosphodiesterase type 5 (PDE5) inhibitor, and offers a rapid onset of action (15 minutes). Its real-world data, including treatment satisfaction, are still lacking.</p><p><strong>Aim: </strong>The study sought to investigate the treatment outcomes of avanafil and the factors impacting treatment satisfaction in a real-world setting.</p><p><strong>Methods: </strong>Between November 2021 and February 2023, erectile dysfunction (ED) patients prescribed avanafil were consecutively enrolled in this phase 4, open-label, cross-sectional, observational study. At each follow-up visit (4-week intervals), participants completed a questionnaire for assessing the use and treatment-emergent adverse events of avanafil, ED severity, and treatment satisfaction.</p><p><strong>Outcomes: </strong>The outcome measures included the Sexual Health Inventory for Men (SHIM), and Erectile Dysfunction Inventory of Treatment Satisfaction.</p><p><strong>Results: </strong>Among 234 patients enrolled, 112 (47.9%) patients had follow-up visits and answered the questionnaire. Treatment with avanafil significantly improved the mean SHIM total score from 10.2 ± 5.6 at baseline to 17.5 ± 6.2 (<i>P</i> < .001). Of the patients treated with avanafil, 71.4% (n = 80 of 112) reported a >4-point improvement in the SHIM total score, and 33.1% (n = 37 of 112) reported normal erectile function. The proportion of patients satisfied with avanafil treatment (defined as Erectile Dysfunction Inventory of Treatment Satisfaction index score ≥60) was 87.5%. Several physical factors (younger age, lower waist circumference, and lower level of low-density lipoprotein), and sexual function factors (shorter duration of ED, higher SHIM total score at baseline, PDE5 inhibitor treatment naive, and acquired premature ejaculation) tended to contribute to satisfaction with avanafil treatment. Treatment-emergent adverse events occurred in 41.1% of patients, and all were mild in severity.</p><p><strong>Clinical implications: </strong>This study identifies the factors associated with treatment satisfaction of avanafil, which may ultimately lead to better treatment outcomes.</p><p><strong>Strengths and limitations: </strong>This is the first study to provide real-world evidence of avanafil for ED treatment, and validated questionnaires were used to assess erectile function and treatment satisfaction. However, the limitations of this study include single-center observational study design, small sample size, and short-term follow-up.</p><p><strong>Conclusion: </strong>Avanafil is an effective treatment for ED, and satisfaction rate is high in an outpatient setting. 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引用次数: 0
摘要
背景:阿伐那非是第二代5型磷酸二酯酶(PDE5)抑制剂,起效迅速(15分钟)。目的:本研究旨在调查阿伐那非的治疗效果以及影响治疗满意度的因素:方法:在2021年11月至2023年2月期间,开具阿伐那非处方的勃起功能障碍(ED)患者被连续纳入这项第4期开放标签横断面观察性研究。在每次随访(间隔4周)时,参与者填写一份问卷,以评估阿伐那非的使用情况和治疗中出现的不良反应、ED严重程度以及治疗满意度:结果:结果测量包括男性性健康量表(SHIM)和勃起功能障碍治疗满意度量表:在 234 名患者中,112 名(47.9%)患者接受了随访并回答了问卷。接受阿伐那非治疗后,平均SHIM总分从基线时的10.2±5.6分大幅提高到17.5±6.2分(P 4分),33.1%的患者(112人中有37人)表示勃起功能正常。对阿伐那非治疗满意的患者比例(定义为勃起功能障碍治疗满意度量表指数得分≥60)为87.5%。一些身体因素(年龄较小、腰围较小、低密度脂蛋白水平较低)和性功能因素(ED持续时间较短、基线时SHIM总分较高、PDE5抑制剂治疗幼稚、获得性早泄)往往有助于提高阿伐那非治疗的满意度。41.1%的患者出现了治疗突发不良事件,且所有不良事件的严重程度都较轻:临床意义:本研究确定了与阿伐那非治疗满意度相关的因素,这可能最终带来更好的治疗效果:这项研究首次提供了阿伐那非治疗ED的实际证据,并使用了有效问卷来评估勃起功能和治疗满意度。然而,这项研究的局限性包括:单中心观察研究设计、样本量小以及短期随访:结论:阿伐那非是治疗 ED 的有效方法,门诊患者的满意度很高。结论:阿伐那非是治疗ED的有效方法,在门诊患者中满意度较高。认识到与患者满意度相关的因素可改善治疗效果。
A real-world pilot study assessing treatment satisfaction with avanafil in patients with erectile dysfunction.
Background: Avanafil is a second-generation phosphodiesterase type 5 (PDE5) inhibitor, and offers a rapid onset of action (15 minutes). Its real-world data, including treatment satisfaction, are still lacking.
Aim: The study sought to investigate the treatment outcomes of avanafil and the factors impacting treatment satisfaction in a real-world setting.
Methods: Between November 2021 and February 2023, erectile dysfunction (ED) patients prescribed avanafil were consecutively enrolled in this phase 4, open-label, cross-sectional, observational study. At each follow-up visit (4-week intervals), participants completed a questionnaire for assessing the use and treatment-emergent adverse events of avanafil, ED severity, and treatment satisfaction.
Outcomes: The outcome measures included the Sexual Health Inventory for Men (SHIM), and Erectile Dysfunction Inventory of Treatment Satisfaction.
Results: Among 234 patients enrolled, 112 (47.9%) patients had follow-up visits and answered the questionnaire. Treatment with avanafil significantly improved the mean SHIM total score from 10.2 ± 5.6 at baseline to 17.5 ± 6.2 (P < .001). Of the patients treated with avanafil, 71.4% (n = 80 of 112) reported a >4-point improvement in the SHIM total score, and 33.1% (n = 37 of 112) reported normal erectile function. The proportion of patients satisfied with avanafil treatment (defined as Erectile Dysfunction Inventory of Treatment Satisfaction index score ≥60) was 87.5%. Several physical factors (younger age, lower waist circumference, and lower level of low-density lipoprotein), and sexual function factors (shorter duration of ED, higher SHIM total score at baseline, PDE5 inhibitor treatment naive, and acquired premature ejaculation) tended to contribute to satisfaction with avanafil treatment. Treatment-emergent adverse events occurred in 41.1% of patients, and all were mild in severity.
Clinical implications: This study identifies the factors associated with treatment satisfaction of avanafil, which may ultimately lead to better treatment outcomes.
Strengths and limitations: This is the first study to provide real-world evidence of avanafil for ED treatment, and validated questionnaires were used to assess erectile function and treatment satisfaction. However, the limitations of this study include single-center observational study design, small sample size, and short-term follow-up.
Conclusion: Avanafil is an effective treatment for ED, and satisfaction rate is high in an outpatient setting. The awareness of identified factors related to patient satisfaction may improve treatment outcomes.
期刊介绍:
Sexual Medicine is an official publication of the International Society for Sexual Medicine, and serves the field as the peer-reviewed, open access journal for rapid dissemination of multidisciplinary clinical and basic research in all areas of global sexual medicine, and particularly acts as a venue for topics of regional or sub-specialty interest. The journal is focused on issues in clinical medicine and epidemiology but also publishes basic science papers with particular relevance to specific populations. Sexual Medicine offers clinicians and researchers a rapid route to publication and the opportunity to publish in a broadly distributed and highly visible global forum. The journal publishes high quality articles from all over the world and actively seeks submissions from countries with expanding sexual medicine communities. Sexual Medicine relies on the same expert panel of editors and reviewers as The Journal of Sexual Medicine and Sexual Medicine Reviews.